HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(1-Methylpiperidin-4-yloxy)-3-trifluoromethylbenzonitrile → HCID 67500259, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(1-Methylpiperidin-4-yloxy)-3-trifluoromethylbenzonitrile | HCID 23145940 | — |
| Reactant | HCID 58629100 | HCID 58629100 | — |
| Product | HCID 67500259 | HCID 67500259 | — |
Reaction Steps
The title compound was synthesized according to the procedure described for the synthesis of 1-[6-(2,2,2-trifluoroethoxy)pyridin-3-yl]ethanamine, step B, starting from 4-[(1-methylpiperidin-4-yl)oxy]-3-(trifluoromethyl)benzonitrile. Yield 49 mg, 62% (oil) after column chromatography on silica gel (eluent: CHCl3/MeOH/conc.NH3, 80:20:1). MS (APCI) m/z 303 [M+H]. 1H NMR (400 MHz, DMSO-D6) δ ppm 1.23 (d, J=6.5 Hz, 3 H), 1.64-1.72 (m, 2 H), 1.86-1.92 (m, 2 H), 2.17 (s, 3 H), 2.21-2.27 (m, 2 H), 2.47-2.55 (m, partly overlapped with DMSO peaks, 2 H), 3.97-4.02 (m, 1 H), 4.55-4.60 (m, 1 H), 7.21 (d, J=8.9 Hz, 1 H), 7.55 (dd, J=8.7, 1.9 Hz, 1 H), 7.60 (d, J=2.0 Hz, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08168668B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-119f38af6e2141f8989157cc78bc5d84 |
| Source note | uspto-grants-2012_05 |